Structural basis for stabilization of the tau pre-mRNA splicing regulatory element by novantrone (mitoxantrone).

Abstract

Some familial neurodegenerative diseases are associated with mutations that destabilize a putative stem-loop structure within an intronic region of the tau pre-messenger RNA (mRNA) and alter the production of tau protein isoforms by alternative splicing. Because stabilization of the stem loop reverses the splicing pattern associated with neurodegeneration, small molecules that stabilize this stem loop would provide new ways to dissect the mechanism of neurodegeneration and treat tauopathies. The anticancer drug mitoxantrone was recently identified in a high throughput screen to stabilize the tau pre-mRNA stem loop. Here we report the solution structure of the tau mRNA-mitoxantrone complex, validated by the structure-activity relationship of existing mitoxantrone analogs. The structure describes the molecular basis for their interaction with RNA and provides a rational basis to optimize the activity of this new class of RNA-binding molecules.

• Authors: Suxin Zheng, Yu Chen, Christine P Donahue, Michael S Wolfe, Gabriele Varani
• Journal: Chemistry & biology (Chem Biol) Vol. 16 Issue 5 Pg. 557-66 (May 29 2009) ISSN: 1879-1301 [Electronic] United States
• PMID: 19477420 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Antineoplastic Agents
• Protein Isoforms
• RNA Precursors
• RNA, Messenger
• tau Proteins
• Mitoxantrone

Topics

• Antineoplastic Agents (chemistry, pharmacology)
• Base Sequence
• Mitoxantrone (chemistry, pharmacology)
• Protein Isoforms (genetics, metabolism)
• RNA Precursors (chemistry, metabolism)
• RNA Splicing
• RNA, Messenger (chemistry, metabolism)
• Structure-Activity Relationship
• tau Proteins (genetics, metabolism)